Akar N - Search Results

1

The role of plasminogen activator inhibitor-1 polymorphism, factor-V-Leiden, and prothrombin-20210 mutations in pulmonary thromboembolism.

Oguzulgen IK, Yilmaz E, Demirtas S, Erkekol FO, Ekim N, Demir N, Numanoglu N, Ozel D, Ulu A, Akar N. Oguzulgen IK, et al. Among authors: akar n. Clin Appl Thromb Hemost. 2009 Feb;15(1):73-7. doi: 10.1177/1076029607305110. Epub 2007 Dec 26. Clin Appl Thromb Hemost. 2009. PMID: 18160588 Free article.

2

Search for genetic factors favoring thrombosis in Turkish population.

Akar N, Akar E, Misirlioğlu M, Avcu F, Yalçin A, Cin S. Akar N, et al. Among authors: akar e. Thromb Res. 1998 Oct 15;92(2):79-82. doi: 10.1016/s0049-3848(98)00113-3. Thromb Res. 1998. PMID: 9792115

3

Factor V (His 1299 Arg) in Turkish patients with venous thromboembolism.

Akar N, Akar E, Yilmaz E. Akar N, et al. Among authors: akar e. Am J Hematol. 2000 Feb;63(2):102-3. doi: 10.1002/(sici)1096-8652(200002)63:2<102::aid-ajh10>3.0.co;2-r. Am J Hematol. 2000. PMID: 10629579 Free article. No abstract available.

4

Effect of plasminogen activator inhibitor-1 4G/5G polymorphism in Turkish deep vein thrombotic patients with and without FV1691 G-A.

Akar N, Yilmaz E, Akar E, Avcu F, Yalçin A, Cin S. Akar N, et al. Among authors: akar e. Thromb Res. 2000 Feb 15;97(4):227-30. doi: 10.1016/s0049-3848(99)00164-4. Thromb Res. 2000. PMID: 10674409

5

Prothrombin gene 20210 G-->A and Factor V Arg 506 to Gln mutation in a patient with Buerger's disease--a case report.

Avcu F, Akar N, Akar E, Beyan C, Yalçin A. Avcu F, et al. Among authors: akar e, akar n. Angiology. 2000 May;51(5):421-3. doi: 10.1177/000331970005100509. Angiology. 2000. PMID: 10826859

6

Coexistence of factor V 1691 G-A and factor V 4070 A-G mutation in turkish thromboembolic patients.

Akar N, Akar E, Yilmaz E. Akar N, et al. Among authors: akar e. Am J Hematol. 2000 Sep;65(1):88. doi: 10.1002/1096-8652(200009)65:1<88::aid-ajh19>3.0.co;2-0. Am J Hematol. 2000. PMID: 10936874 Free article. No abstract available.

7

Factor V (His 1299 Arg) in young Turkish patients with cerebral infarct.

Akar N, Yilmaz E, Akar E, Deda G, Sipahi T. Akar N, et al. Among authors: akar e. Haemostasis. 2000 May-Jun;30(3):118-22. doi: 10.1159/000022533. Haemostasis. 2000. PMID: 11014961

8

The role of prothrombotic mutations in patients with Buerger's disease.

Avcu F, Akar E, Demirkiliç U, Yilmaz E, Akar N, Yalçin A. Avcu F, et al. Among authors: akar e, akar n. Thromb Res. 2000 Nov 1;100(3):143-7. doi: 10.1016/s0049-3848(00)00310-8. Thromb Res. 2000. PMID: 11108900

9

Methylenetetrahydrofolate reductase gene polymorphism and risk of premature myocardial infarction.

Gülec S, Aras O, Akar E, Tutar E, Omürlü K, Avci F, Dinçer I, Akar N, Oral D. Gülec S, et al. Among authors: akar e, akar n. Clin Cardiol. 2001 Apr;24(4):281-4. doi: 10.1002/clc.4960240405. Clin Cardiol. 2001. PMID: 11303694 Free PMC article.

10

Common mutations at the homocysteine metabolism pathway and pediatric stroke.

Akar N, Akar E, Ozel D, Deda G, Sipahi T. Akar N, et al. Among authors: akar e. Thromb Res. 2001 Apr 15;102(2):115-20. doi: 10.1016/s0049-3848(01)00226-2. Thromb Res. 2001. PMID: 11323021

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